Canonical Allele Identifier: CA368368884

Gene: CYP3A4

Linked Data

• dbSNP Id: rs1235985595
• gnomAD v2: 7-99359704-G-T
• gnomAD v4: 7-99762081-G-T
• MyVariant Identifiers: chr7:g.99359704G>T (hg19) ; chr7:g.99762081G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.99762081G>T , CM000669.2:g.99762081G>T	GRCh38
NC_000007.13:g.99359704G>T , CM000669.1:g.99359704G>T	GRCh37
NC_000007.12:g.99197640G>T	NCBI36
NG_008421.1:g.27105C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000336411.7:c.1213C>A	ENSP00000337915.3:p.Pro405Thr
ENST00000651162.1:n.648C>A
ENST00000651514.1:c.1213C>A MANE Select	ENSP00000498939.1:p.Pro405Thr
ENST00000651783.1:c.754C>A	ENSP00000498924.1:p.Pro252Thr
ENST00000652018.1:c.1066C>A	ENSP00000498733.1:p.Pro356Thr
ENST00000336411.6:c.1213C>A	ENSP00000337915.2:p.Pro405Thr
ENST00000354593.6:c.763C>A	ENSP00000346607.2:p.Pro255Thr
NM_001202855.2:c.1210C>A	NP_001189784.1:p.Pro404Thr
NM_017460.5:c.1213C>A	NP_059488.2:p.Pro405Thr
XM_011515841.1:c.1213C>A	XP_011514143.1:p.Pro405Thr
XM_011515842.1:c.1210C>A	XP_011514144.1:p.Pro404Thr
NM_017460.6:c.1213C>A MANE Select	NP_059488.2:p.Pro405Thr
NM_001202855.3:c.1210C>A	NP_001189784.1:p.Pro404Thr